Detalhe da pesquisa
1.
Challenges and needs in cerebrovascular disease pathway: A qualitative descriptive study from the patients' and healthcare professionals' perspectives.
J Adv Nurs
; 2024 Jan 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-38214101
2.
Patient experiences on the quality of cerebrovascular diseases counselling using digital solutions in hospital-A qualitative research study.
J Clin Nurs
; 33(6): 2259-2273, 2024 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-38413773
3.
Validation of the Finnish Version of the Unified Dyskinesia Rating Scale.
Eur Neurol
; 84(6): 444-449, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-34261060
4.
Efficacy and safety of fremanezumab in patients with migraine and inadequate response to prior preventive treatment: subgroup analyses by country of a randomized, placebo-controlled trial.
J Headache Pain
; 22(1): 26, 2021 Apr 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-33863272
5.
Impact of age and sex on the efficacy of fremanezumab in patients with difficult-to-treat migraine: results of the randomized, placebo-controlled, phase 3b FOCUS study.
J Headache Pain
; 22(1): 152, 2021 Dec 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-34922436
6.
Screening for Fabry disease and Hereditary ATTR amyloidosis in idiopathic small-fiber and mixed neuropathy.
Muscle Nerve
; 59(3): 354-357, 2019 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-30246259
7.
Heterozygous SSBP1 start loss mutation co-segregates with hearing loss and the m.1555A>G mtDNA variant in a large multigenerational family.
Brain
; 141(1): 55-62, 2018 01 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29182774
8.
Variants p.Q1236H and p.E1143G in mitochondrial DNA polymerase gamma POLG1 are not associated with increased risk for valproate-induced hepatotoxicity or pancreatic toxicity: A retrospective cohort study of patients with epilepsy.
Epilepsia
; 59(11): 2125-2136, 2018 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-30255931
9.
Mutation m.15923A>G in the MT-TT gene causes mild myopathy - case report of an adult-onset phenotype.
BMC Neurol
; 18(1): 149, 2018 Sep 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-30236074
10.
A novel MTTT mutation m.15933G > A revealed in analysis of mitochondrial DNA in patients with suspected mitochondrial disease.
BMC Med Genet
; 18(1): 14, 2017 Feb 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-28187756
11.
Molecular Epidemiology of Charcot-Marie-Tooth Disease in Northern Ostrobothnia, Finland: A Population-Based Study.
Neuroepidemiology
; 49(1-2): 34-39, 2017.
Artigo
em Inglês
| MEDLINE | ID: mdl-28810241
12.
Case report: a novel frameshift mutation in the mitochondrial cytochrome c oxidase II gene causing mitochondrial disorder.
BMC Neurol
; 17(1): 96, 2017 May 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-28521807
13.
Myocardial glucose uptake in patients with the m.3243A > G mutation in mitochondrial DNA.
J Inherit Metab Dis
; 39(1): 67-74, 2016 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-26112752
14.
Atypical phenotypes in titinopathies explained by second titin mutations.
Ann Neurol
; 75(2): 230-40, 2014 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-24395473
15.
Hereditary myopathy with early respiratory failure: occurrence in various populations.
J Neurol Neurosurg Psychiatry
; 85(3): 345-53, 2014 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-23606733
16.
Status epilepticus in POLG disease: a large multinational study.
J Neurol
; 2024 Jun 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-38822839
17.
Feasibility and patient acceptability of a commercially available wearable and a smart phone application in identification of motor states in parkinson's disease.
PLOS Digit Health
; 2(4): e0000225, 2023 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-37027348
18.
Phenotype of Patients With Charcot-Marie-Tooth With the p.His123Arg Mutation in GDAP1 in Northern Finland.
Neurol Genet
; 7(6): e629, 2021 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-34632054
19.
Long-term effectiveness and safety of lemborexant in adults with insomnia disorder: results from a phase 3 randomized clinical trial.
Sleep Med
; 80: 333-342, 2021 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-33636648
20.
POLG1 p.R722H mutation associated with multiple mtDNA deletions and a neurological phenotype.
BMC Neurol
; 10: 29, 2010 May 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-20438629